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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ITGA2B
(Q837H)
Single nucleotide variant
(missense variant)
Glanzmann thrombasthenia
GBenign
ITGA2B
Deletion
(intron variant)
Glanzmann thrombasthenia
GBenign